POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 12000 MW)
Substance profile for UNII WE369X5600, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.
Substance Identity#
- UNII
- WE369X5600
- Preferred term
- POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 12000 MW)
- Registry number
- 26780-50-7
- Ingredient type
- INGREDIENT SUBSTANCE
- Molecular formula
- Polymer substance not supported
Chemical And Database Identifiers#
- RxCUI
- 1536460
- PubChem
- 0
- INN ID
- 0
Open Chemistry Sources#
| Source | Identifier | Link |
|---|---|---|
| RxNorm | 1536460 |  mor.nlm.nih.gov/RxNav/search?searchBy=RXCUI&searchTerm=1536460 |
| FDA Substance Registration System | WE369X5600 |  precision.fda.gov/uniisearch/srs/unii/WE369X5600 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 12000 MW) | INACTIVE INGREDIENT | WE369X5600 | PROPEL () KIT PROPEL MINI () KIT [INTERSECT ENT, INC.] | 3 | |
| POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 12000 MW) | INACTIVE INGREDIENT | WE369X5600 | SIGNIFOR LAR (PASIREOTIDE) KIT [NOVARTIS PHARMACEUTICALS CORPORATION] | 2 |
Inactive Ingredient Database#
| Ingredient | UNII | CAS | Dosage form | Route | Potency | Maximum daily exposure |
|---|---|---|---|---|---|---|
| DL-LACTIDE AND GLYCOLIDE (50:50) COPOLYMER 12000 ACID | WE369X5600 | 26780507 | IMPLANT | ENDOSINUSIAL | 1.35 mg | |
| DL-LACTIDE AND GLYCOLIDE (50:50) COPOLYMER 12000 ACID | WE369X5600 | 26780507 | IMPLANT | INTRAVITREAL | 1 mg | |
| DL-LACTIDE AND GLYCOLIDE (50:50) COPOLYMER 12000 ACID | WE369X5600 | 26780507 | INJECTION, SOLUTION | SUBCUTANEOUS | 533 mg |